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2023, Journal of Marine Science and Engineering
Coastal wetlands are valuable and sensitive environments that are among the most productive yet highly threatened systems in the world. They are typically located in areas where freshwater and saltwater mix, such as estuaries, lagoons, deltas, and have many forms, including mangrove forests, salt marshes, seagrass beds and tidal flats . These ecosystems are characterized by a unique combination of hydrology, soil conditions, and vegetation that allows them to thrive in the harsh coastal environment. The complexity of coastal wetland systems can be better understood within the context of the biogeomorphology that includes the coastal landscapes of which they are a part. They provide numerous ecosystem services, including habitats for wildlife, water filtration, carbon sequestration, and storm protection . One of the most important roles of wetlands is the regulation of global climate change through sequestering and releasing a major proportion of fixed carbon in the biosphere. Global climate change is expected to exacerbate the loss and degradation of many coastal wetlands and the loss or decline of their species and to harm the human populations dependent on their services; however, projections about the extent of such loss and degradation or decline are not yet well-established. The Special Issue "Coastal Wetlands" includes eight contributions published during 2020-2022. The contributions can be subdivided into the following subjects: cartography, carbon sequestration, halophytic vegetation and impacts of global climate change. Historical mapping provides very valuable information for the understanding of the geomorphological evolution of the coastal wetlands, and, in most cases, it represents the first step in the analysis of coastal processes . Piccardi et al. (2020) [3] have carried out an interesting study on the historical evolution (16th-20th Century) of Cispatá Bay and Mestizos (Colombian Caribbean coast) from ancient documents and maps. They have had to review about 500 manuscripts or printed maps produced from the 16th century to 1937, time when the Tinajones delta was formed in the mouth of Sinu River. Some cartographies were georeferenced, and others were visually analyzed. The analysis of all the documents clarifies the evolution of this coastal stretch and allows establishing a new reconstruction of the formation stages of Cispatá bay. Carbon sequestration is one of the most important ecosystem services provided by coastal wetlands. Coastal wetlands can capture carbon dioxide (CO 2 ) from the atmosphere and store it in plants and in the soil, helping to mitigate the effects of climate change. Coastal wetlands are among the most effective natural carbon sinks on the planet, removing up to 10 times more carbon per unit area than tropical rainforests . Mao et al. (2021) [5] measured total organic carbon (TOC), total nitrogen (TN), and stable carbon isotopes (δ 13 C), in surface sediments from vegetated intertidal saltmarsh areas and bare tidal flat sediments near (BF1) and far (BF2) from the vegetated areas, along the Rudong Coast (eastern coast of China). These observations were used to explore the spatial distribution of organic carbon in different depositional environments. The distribution and sources of organic carbon were examined under different depositional environments based on C/N ratios and a two-terminal mixing model. The results showed that the organic carbon content of the vegetated saltmarsh sediment is higher than that of the bare tidal flat areas, with the tidal flat sediments nearer to the vegetated area (BF1) having a relatively
Biogeosciences, 2014
Studies on carbon stock in salt marsh sediments have increased since the review by Chmura et al. (2003). However, uncertainties exist in estimating global carbon storage in these vulnerable coastal habitats, thus hindering the assessment of their importance. Combining direct data and indirect estimation, this study compiled studies involving 143 sites across the Southern and Northern hemispheres, and provides an updated estimate of the global average carbon accumulation rate (CAR) at 244.7 g Cm−2 yr−1 in salt marsh sediments. Based on region-specific CAR and estimates of salt marsh area in various geographic regions between 40 S to 69.7 N, total CAR in global salt marsh sediments is estimated at 10.2 TgC yr−1. Latitude, tidal range and elevation appear to be important drivers for CAR of salt marsh sediments, with considerable variation among different biogeographic regions. The data indicate that while the capacity for carbon sequestration by salt marsh sediments ranked the first amongst coastal wetland and forested terrestrial ecosystems, their carbon budget was the smallest due to their limited and declining global areal extent. However, some uncertainties remain for our global estimate owing to limited data availability.
Nature Communications, 2020
Tidal wetlands are global hotspots of carbon storage but errors exist with current estimates on their carbon density due to the use of factors estimated from other habitats for converting loss-on-ignition (LOI) to organic carbon (OC); and the omission of certain significant carbon pools. Here we show that the widely used conversion factor (LOI/OC = 1.724) is significantly lower than our measurements for saltmarsh sediments (1.92 ± 0.01) and oversimplifies the polynomial relationship between sediment OC and LOI for mangrove forests. Global man- grove OC stock in the top-meter sediment reaches 1.93 Pg when corrected for this bias, and is 20% lower than the previous estimates. Ecosystem carbon stock (living and dead biomass, sediment OC and inorganic carbon) is estimated at 3.7 – 6.2 Pg. Mangrove deforestation leads to carbon emission rates at 23.5 – 38.7 Tg yr−1 after 2000. Mangrove sediment OC stock has previously been over-estimated while ecosystem carbon stock underestimated.
Global Biogeochemical Cycles, 2003
Wetlands represent the largest component of the terrestrial biological carbon pool, and thus play an important role in global carbon cycles. Most global carbon budgets however, have focused on dry land ecosystems that extend over large areas, and have not accounted for the many small, scattered carbon-storing ecosystems such as tidal saline wetlands. We compiled data for 154 sites in mangroves and salt marshes from the western and eastern Atlantic and Pacific coasts, as well as the Indian Ocean, Mediterranean Ocean, and Gulf of Mexico. The set of sites spans a latitudinal range from 22.4°S in the Indian Ocean to 55.5°N in the northeastern Atlantic. The average soil C density of mangrove swamps (0.055 ± 0.004 g cm -3 ) is significantly higher than the salt marsh average (0.039 ± 0.003 g cm -3 ). Soil C density in mangrove swamps and Spartina patens marshes declines with increasing average annual temperature, probably due to increased decay rates at higher temperatures. In contrast, carbon sequestration rates were not significantly different between mangrove swamps and salt marshes. Variability in sediment accumulation rates within marshes is a major control of carbon sequestration rates masking any relationship with climatic parameters. Globally, these combined wetlands store at least 44.6 Tg C yr -1 , and probably more as detailed areal inventories are not available for salt marshes in China and South America. Much attention has been given to the role of freshwater wetlands, particularly northern peatlands, as carbon sinks. In contrast to peatlands, salt marshes and mangroves release negligible amounts of greenhouse gases and store more carbon per unit area.
Despite their small area, tidal wetlands and estuaries influence both terrestrial and oceanic carbon stocks and fluxes at global scales. 2. Carbon fluxes in tidal wetlands and estuaries are strongly influenced by land-use decisions upstream, as associated with nutrients, sediments, and hydrology. 3. Carbon fluxes in tidal wetlands and estuaries are strongly influenced by physical, chemical and biological coastal ocean processes 4. Estuaries vary in their relative distribution of tidal and subtidal components, thus influencing the direction and magnitude of C related exchanges between tidal wetlands and estuarine waters.
Estuaries and Coasts
Salt marshes provide the important ecosystem service of carbon storage in their sediments; however, little is known about the sources of such carbon and whether they differ between historically unaltered and restoring systems. In this study, stable isotope analysis was used to quantify carbon sources in a restoring, sparsely vegetated marsh (Restoring) and an adjacent, historically unaltered marsh (Reference) in the Nisqually River Delta (NRD) of Washington, USA. Three sediment cores were collected at "Inland" and "Seaward" locations at both marshes~6 years after restoration. Benthic diatoms, C3 plants, C4 plants, and particulate organic matter (POM) were collected throughout the NRD. δ 13 C and δ 15 N values of sources and sediments were used in a Bayesian stable isotope mixing model to determine the contribution of each carbon source to the sediments of both marshes. Autochthonous marsh C3 plants contributed 73 ± 10% (98 g C m −2 year −1) and 89 ± 11% (119 g C m −2 year −1) to Reference-Inland and Reference-Seaward sediment carbon sinks, respectively. In contrast, the sediment carbon sink at the Restoring Marsh received a broad assortment of predominantly allochthonous materials, which varied in relative contribution based on source distance and abundance. Marsh POM contributed the most to Restoring-Seaward (42 ± 34%) (69 g C m −2 year −1) followed by Riverine POM at Restoring-Inland (32 ± 41%) (52 g C m −2 year −1). Overall, this study demonstrates that largely unvegetated, restoring marshes can accumulate carbon by relying predominantly on allochthonous material, which comes mainly from the most abundant and closest estuarine sources.
Maritime Studies, 2019
The atmosphere and the ocean exchange gases resulting in an overall absorption of CO 2 in the ocean Burning fossil fuels, industry and changes in land uses (deforestation, landfill , fires and/or agriculture), and respiration by humans and animals releases extra CO 2 and CH 4 to the atmosphere Plants within terrestrial forests, tidal marsh, mangrove and seagrass ecosystems sequester CO 2 through photosynthesis, which accumulates in their biomass and soils CO 2 , CH 4 CO 2 , CH 4 CO 2 CO 2 CO 2 CO 2 CO 2 CO 2 CO 2 CO 2 Photosynthesis by plankton in the ocean sequester Export of plant and macroalgal biomass in the deep ocean sequesters CO 2 FIGURE 28.1 Conceptual diagram of carbon sequestration by blue carbon ecosystems and some of the activities that influence CO 2 exchange among the atmosphere, soil, and ocean in coastal areas and the open ocean. The major global C pools include the atmosphere, oceans, fossil fuels, vegetation, soils, and detritus. Landfill, smokestacks, cattle farming, and other human activities result in additional methane (CH 4) emissions. 28. CONSERVATION OF BLUE CARBON ECOSYSTEMS FOR CLIMATE CHANGE 966 VII. COASTAL WETLAND SUSTAINABILITY seagrass ecosystems occupying less than 0.2% of the seabed area, they contribute nearly 50% of the CO 2 sequestration in marine sediments, and their C sequestration rates exceed those in the soils of many terrestrial ecosystems by 30-to 50-fold (Chmura et al., 2003; Duarte et al. 2005, 2013; Mcleod et al., 2011). Most macroalgal communities grow on rocky substrate and do not form significant in situ sedimentary C deposits, but the initial estimates of the amount of macroalgae C sequestered in sediments and deep-sea waters suggest that it is comparable to the C sequestered by all other BC ecosystems combined (Krause-Jensen and Duarte, 2016). Furthermore, the C captured by BC ecosystems is stored in marine soils for millennia, rather than the decades or centuries typical of terrestrial forests. This is due in part to the high rates of vertical accretion in tidal marsh, mangrove, and seagrass ecosystems, ranging from 0.4 to 21 mm year À1 (Mateo et al., 1997; McKee et al., 2007; Duarte et al., 2013). This process of raising the seafloor is driven partly through the trapping and settling of particles from the water column and partly through organic matter production. This acts to bury the C in anoxic conditions, thereby slowing down its remineralization by microbes (Krauss et al., 2014; Mateo et al., 2006; Pedersen et al., 2011). Globally, tidal marsh, mangrove, and seagrass ecosystems sequester annually a similar amount of C to terrestrial forests, despite their extent being less than 3% of that of forests (Duarte et al., 2013). Unlike terrestrial forests, mangroves and tidal marshes rarely burn in wildfires, although they are exposed to other disturbances (e.g., tropical storms). BC ecosystems provide important and valuable ecosystem services critical for climate change mitigation and adaptation, including coastal protection from storms and shoreline erosion, regulation of water quality, provision of habitat for commercially important fisheries and enhancing biodiversity, and being globally significant C sinks (
Wetlands, 2017
Across the globe, coastal wetland vegetation distributions are changing in response to climate change. In the southeastern United States, increased winter temperatures have resulted in poleward range expansion of mangroves into pure salt marsh habitat. Climate change-induced expansion of mangroves into salt marsh will significantly alter carbon (C) storage capacity of these wetlands, which currently store the highest average C per land area among unmanaged terrestrial ecosystems. Total ecosystem C stocks were measured along a 342 km latitudinal gradient of mangrovetomarsh dominance in Florida. Carbon stocks were quantified through measurements of above-and belowground biomass and soil C. Interior mangrove C stocks were greater than both salt marsh and ecotonal C stocks and soil C comprised the majority of each ecosystem C component (51-98%). The wetlands investigated in this study cover 38,532 ha, and store an average of 215 Mg of C ha −1. Currently, mangroves cover 31% of the land area studied, storing 44% of the total C, whereas salt marshes occupy 68% of the wetland area and only store 55% of the C. Total conversion of salt marsh to mangrove may increase C storage by 26%, predominately due to increases in aboveground biomass.
Proceedings of the National Academy of Sciences of the United States of America, 2016
Given their relatively small area, mangroves and their organic sediments are of disproportionate importance to global carbon sequestration and carbon storage. Peat deposition and preservation allows some mangroves to accrete vertically and keep pace with sea-level rise by growing on their own root remains. In this study we show that mangroves in desert inlets in the coasts of the Baja California have been accumulating root peat for nearly 2,000 y and harbor a belowground carbon content of 900-34,00 Mg C/ha, with an average value of 1,130 (± 128) Mg C/ha, and a belowground carbon accumulation similar to that found under some of the tallest tropical mangroves in the Mexican Pacific coast. The depth-age curve for the mangrove sediments of Baja California indicates that sea level in the peninsula has been rising at a mean rate of 0.70 mm/y (± 0.07) during the last 17 centuries, a value similar to the rates of sea-level rise estimated for the Caribbean during a comparable period. By accr...
Nature, 2019
Coastal wetlands (mangrove, tidal marsh and seagrass) sustain the highest rates of carbon sequestration per unit area of all natural systems 1,2 , primarily because of their comparatively high productivity and preservation of organic carbon within sedimentary substrates 3. Climate change and associated relative sea-level rise (RSLR) have been proposed to increase the rate of organic-carbon burial in coastal wetlands in the first half of the twenty-first century 4 , but these carbon-climate feedback effects have been modelled to diminish over time as wetlands are increasingly submerged and carbon stores become compromised by erosion 4,5. Here we show that tidal marshes on coastlines that experienced rapid RSLR over the past few millennia (in the late Holocene, from about 4,200 years ago to the present) have on average 1.7 to 3.7 times higher soil carbon concentrations within 20 centimetres of the surface than those subject to a long period of sea-level stability. This disparity increases with depth, with soil carbon concentrations reduced by a factor of 4.9 to 9.1 at depths of 50 to 100 centimetres. We analyse the response of a wetland exposed to recent rapid RSLR following subsidence associated with pillar collapse in an underlying mine and demonstrate that the gain in carbon accumulation and elevation is proportional to the accommodation space (that is, the space available for mineral and organic material accumulation) created by RSLR. Our results suggest that coastal wetlands characteristic of tectonically stable coastlines have lower carbon storage owing to a lack of accommodation space and that carbon sequestration increases according to the vertical and lateral accommodation space 6 created by RSLR. Such wetlands will provide long-term mitigating feedback effects that are relevant to global climate-carbon modelling. Broad biogeographic drivers, such as vegetation, climate, topography or water chemistry, are often emphasized as important global-scale controls on organic matter accumulation, decomposition and carbon stocks within tidal wetlands 7. However, relative sea-level trends over the Holocene varied across the globe, principally on the basis of distance from maximal ice-sheet extent during the last glacial period, and have a profound influence on the contemporary character of coastal wetlands 8,9. In Europe and North America, where studies of coastal wetland sea-level rise (SLR) impacts are concentrated, sea levels have been rising over the past few millennia at a decelerating rate up to the present (Fig. 1a, b). Tidal marshes in these locations, particularly when sediment supply is low-moderate, are often characterized by deep sediments that are highly organic 4,10,11 , in contrast to coastal wetlands in locations where the sea level has been stable for the past few millenia 12 , in spite of similarities in floristics 13. We review published data, contribute new observations on soil carbon concentrations (%C) in tidal-marsh sediments and compare %C values over the active root zone (0-20 cm) and sub-surface depths (20-50 cm, 50-100 cm and >1 m) for 345 locations that vary in rates of SLR over the late Holocene (Supplementary Information). We find that variation in RSLR over past millennia is a primary control on carbon storage. Overall %C varies consistently between RSLR zones (areas spatially
Environmental Research Letters, 2018
Certain coastal ecosystems such as mangrove, saltmarsh and seagrass habitats have been identified as significant natural carbon sinks, through the sequestration and storage of carbon in their biomass and sediments, collectively known as 'blue carbon' ecosystems. These ecosystems can often thrive in extreme environments where terrestrial systems otherwise survive at the limit of their existence, such as in arid and desert regions of the globe. To further our understanding of the capability of blue carbon ecosystems to sequester and store carbon in such extreme climates, we measured carbon sediment stocks in 25 sites along the Western Arabian Gulf coast. While seagrass meadows and saltmarsh habitats were widely distributed along the coast, mangrove stands were much reduced as a result of anthropogenic pressures, with 90% of stands having been lost over the last century. Carbon stocks in 1 m deep surface sediments were similar across all three blue carbon habitats, with comparable stocks for saltmarsh (81 ± 22 Mg C org ha −1), seagrass (76 ± 20 Mg C org ha −1) and mangroves (76 ± 23 Mg C org ha −1). We recorded a 38% decrease in carbon stocks between mature established mangrove stands (91 Mg C org ha −1) and recently planted mangroves (56 Mg C org ha −1). Mangroves also had the lowest carbon stock per total area owing to their very limited spatial coverage along the coast. The largest stock per total area belonged to seagrass beds as a result of their large spatial coverage within the Gulf. We employed 210 Pb dating to determine the sediment accretion rates in each ecosystem and found mangrove habitats to be the most efficient carbon sequesters over the past century, with the highest carbon burial rate of the three ecosystems (19 g C org m −2 yr −1), followed by seagrass (9 g C org m −2 yr −1) and saltmarshes (8 g C org m −2 yr −1). In this work, we describe a comprehensive comparison of sediment stocks in different blue carbon ecosystems within a single marine environment and across a large geographical area, and discuss our results in a global context for other blue carbon ecosystems in the dry tropics.
Current Opinion in Environmental Sustainability, 2012
Coastal vegetated wetlands have recently been identified as very important global C sinks but vulnerable to degradation by direct human alteration of their habitats. While their expanse is small globally, areal rates of C burial, or sequestration, are among the highest of Earth's ecosystems. There is considerable uncertainty in the magnitude of total global sequestration in these systems for two reasons: poor estimates of their global areas and high variability and uncertainty in areal rates of burial between systems. The magnitude of C burial in vegetated coastal systems has been decreasing rapidly over the past century due primarily to human disturbances such as dredging, filling, eutrophication, and timber harvest. These systems continue to be lost globally at rates ranging from 1% to 7% annually. We find that climate change including global warming, human engineering of river systems, continued agricultural expansion, and sea level rise will also negatively impact C burial of coastal vegetated wetlands. A decrease in global C burial in these systems will ultimately exacerbate CO 2 emissions, and further contribute to climate change in the future.
National Science Review, 2020
Coastal tidal wetlands produce and accumulate significant amounts of organic carbon (C) that help to mitigate climate change. However, previous data limitations have prevented a robust evaluation of the global rates and mechanisms driving C accumulation. Here, we go beyond recent soil C stock estimates to reveal global tidal wetland C accumulation and predict changes under relative sea level rise, temperature and precipitation. We use data from literature study sites and our new observations spanning wide latitudinal gradients and 20 countries. Globally, tidal wetlands accumulate 53.65 (95%CI: 48.52–59.01) Tg C yr−1, which is ∼30% of the organic C buried on the ocean floor. Modeling based on current climatic drivers and under projected emissions scenarios revealed a net increase in the global C accumulation by 2100. This rapid increase is driven by sea level rise in tidal marshes, and higher temperature and precipitation in mangroves. Countries with large areas of coastal wetlands, ...
Science of The Total Environment
Coastal vegetated habitats can be important sinks of organic carbon (C org) and mitigate global warming by sequestering significant quantities of atmospheric CO 2 and storing sedimentary C org for long periods, although their C org burial and storage capacity may be affected by ongoing sea level rise and human intervention. Geochemical data from published 210 Pb-dated sediment cores, collected from low-energy microtidal coastal wetlands in El Salvador (Jiquilisco Bay) and in Mexico (Salada Lagoon; Estero de Urias Lagoon; Sian Ka'an Biosphere Reserve) were revisited to assess temporal changes (within the last 100 years) of C org concentrations, storage and burial rates in tropical salt marshes under the influence of sea level rise and contrasting anthropization degree. Grain size distribution was used to identify hydrodynamic changes, and δ 13 C to distinguish terrigenous sediments from those accumulated under the influence of marine transgression. Although the accretion rate ranges in all sediment records were comparable, C org concentrations (0.2-30%), stocks (30-465 Mg ha −1 , by extrapolation to 1 m depth), and burial rates (3-378 g m −2 year −1
Limnology and Oceanography, 1999
Effects of nutrient loading on the carbon balance of coastal wetland sediments Abstract-Results of a 12-yr study in an oligotrophic South Carolina salt marsh demonstrate that soil respiration increased by 795 g C m Ϫ2 yr Ϫ1 and that carbon inventories decreased in sediments fertilized with nitrogen and phosphorus. Fertilized plots became net sources of carbon to the atmosphere, and sediment respiration continues in these plots at an accelerated pace. After 12 yr of treatment, soil macroorganic matter in the top 5 cm of sediment was 475 g C m Ϫ2 lower in fertilized plots than in controls, which is equivalent to a constant loss rate of 40 g C m Ϫ2 yr Ϫ1. It is not known whether soil carbon in fertilized plots has reached a new equilibrium or continues to decline. The increase in soil respiration in the fertilized plots was far greater than the loss of sediment organic matter, which indicates that the increase in soil respiration was largely due to an increase in primary production. Sediment respiration in laboratory incubations also demonstrated positive effects of nutrients. Thus, the results indicate that increased nutrient loading of oligotrophic wetlands can lead to an increased rate of sediment carbon turnover and a net loss of carbon from sediments. Notes an oligotrophic salt marsh has significantly reduced the carbon standing stock and increased the turnover rate of soil carbon, which indicates that increased nutrient loadings could result in a net transfer of soil carbon to the atmosphere from organic-rich soils. This has important implications for global climate, to the extent that eutrophication may alter the carbon balance of wetland soils generally, and for maintenance of coastal wetlands threatened by rising sea level.
Estuarine Coastal and Shelf Science, 1997
Measurements of nitrogen, organic carbon and δ13C are presented forSpartina-dominated marsh sediments from a mineral marsh in SW Netherlands and from a peaty marsh in Massachusetts, U.S.A. δ13C of organic carbon in the peaty marsh sediments is similar to that ofSpartinamaterial, whereas that in mineral marshes is depleted by 9-12‰. It is argued that this depletion in δ13C of organic matter in marsh sediments is due to trapping of allochthonous organic matter which is depleted in13C. The isotopic composition and concentration of organic carbon are used in a simple mass balance to constrain the amount of plant material accumulating in marsh sediments, i.e. in terms of the so-called net ecosystem production. Net ecosystem production (∼2-100 g C m-2year-1) is a small fraction (1-5%) of plant production (∼2000 g C m-2year-1). This small amount of plant material being preserved is nevertheless sufficient to support marsh-accretion rates similar to the rate of sea-level rise.
Frontiers in Ecology and Evolution, 2020
Global Biogeochemical Cycles , 2022
Wetlands are considered to be among the most productive but vulnerable ecosystems (Kirwan & Megonigal, 2013; Su et al., 2021; Wen et al., 2019). Despite covering just 4%-6% of the total land area, wetlands hold approximately 450 Pg of the global soil carbon, representing 25%-30% of the terrestrial biosphere carbon pool (Kayranli et al., 2010). Coastal wetlands are a crucial sink in the global carbon cycle due to high sedimentation rate and burial of organic matter (Drake et al., 2015; Packalen et al., 2014; Zhang, Bai, et al., 2021), and it is estimated that coastal wetlands globally store at least 53.7 Tg C yr −1 (Wang et al., 2021). However, wetland habitats have been impacted around the world, and despite international initiative to protect these habitats (e.g., Ramsar Convention on Wetlands), wetland degradation and loss rate remain high in Asia (Davidson, 2014), potentially altering the land's carbon source-sink dynamics over different time and spatial scales (Mitsch et al., 2013).
Marine Ecology Progress Series, 2019
Blue carbon ecosystems, including salt marshes, play an important role in the global carbon cycle because of their high efficiency to store soil organic carbon (OC). Few studies focus on the origin of OC stored in salt-marsh soils, which comes from either allochthonous or autochthonous sources. The origin, however, has important implications for carbon crediting approaches because the alternative fate of allochthonous OC (AllOC), i.e. if it had not accumulated in the Blue C ecosystem, is unclear. Here, we assessed the origin of OC in two mainland salt-marsh sites of the European Wadden Sea, analyzing δ 13 C of topsoil (0-5 cm) samples, freshly deposited sediment (allochthonous source), and of above-and belowground biomass of vegetation (autochthonous sources). We tested for effects of geomorphological factors, including elevation and the distance to sediment sources, and of livestock grazing, as the most important land-use form, on the relative contributions of allochthonous versus autochthonous sources to the topsoil OC stock. A negative effect of distance to the creek on the relative contribution of AllOC was found at only one of the two salt marshes, probably 2 due to differences in micro-topography between the two salt marshes. Additionally, the relative contribution of AllOC increased with increasing distance to the marsh edge in areas without livestock-grazing, while it decreased in grazed areas. Our findings demonstrate that spatial factors such as surface elevation and distance to a sediment source, which have been found to determine the spatial patterns of sediment deposition, also are important factors determining the relative contribution of AllOC to topsoil OC stocks of salt marshes. Furthermore, we provide first evidence that livestock-grazing can reduce the relative contribution of AllOC to the soil OC stock. These findings thereby yield important implications for C crediting and land-use management.
Journal of Geophysical Research: Biogeosciences
High rates of carbon burial observed in wetland sediments have garnered attention as a potential "natural fix" to reduce the concentration of carbon dioxide (CO 2 ) in Earth's atmosphere. A carbon accumulation rate (CAR) can be determined through various methods that integrate a carbon stock over different time periods, ranging from decades to millennia. Our goal was to assess how CAR changed over the lifespan of a salt marsh. We applied a geochronology to a series of salt marsh cores using both 14 C and 210 Pb markers to calculate CARs that were integrated between 35 and 2,460 years before present. CAR was 39 g C·m −2 ·year −1 when integrated over millennia but was upward of 148 g C·m −2 ·year −1 for the past century. We present additional evidence to account for this variability by linking it to changes in relative sea level rise (RSLR), where higher rates of RSLR were associated with higher CARs. Thus, the CAR calculated for a wetland should integrate timescales that capture the influence of contemporary RSLR. Therefore, caution should be exercised not to utilize a CAR calculated over inappropriately short or long timescales as a current assessment or forecasting tool for the climate change mitigation potential of a wetland.
Current Forestry Reports
Purpose of Review We use the 'seascape' concept to explore how interactions between mangrove forests, tidal marshes and seagrass influence the storage of carbon in these ecosystems. Mangrove forests, with the other two 'blue carbon' habitats, are exceptionally powerful carbon sinks. Maintaining and enhancing these sinks is an emerging priority in climate change mitigation. However, managing any one ecosystem on its own risks is ignoring important contextual drivers of carbon storage emerging from its place in the seascape. We consider how interactions between these coastal habitats directly or indirectly affect the amounts of carbon they can store. Recent Findings The export of carbon from seagrasses may occur over hundreds or thousands of kilometres, much further than reported for mangroves or tidal marshes. Seagrasses may buffer mangroves from wave impacts, assisting forest regeneration. Trophic cascades supported by contiguous blue carbon habitat may limit excessive herbivory and bioturbation in them but evidence is limited. Summary Direct transfers of carbon between blue carbon habitats are common and are likely to enhance total carbon storage, but our understanding of their contribution to carbon stocks at the seascape level is elementary. There is evidence for indirect enhancement of carbon storage at the seascape by close association of habitats, mostly through the creation and maintenance of propitious conditions by one ecosystem for another. Protection from waves of mangroves by seagrass and protection from excess nutrients and sediment of seagrass by mangroves and tidal marsh are key mechanisms. There is little evidence or theory suggesting negative effects on carbon storage of one blue carbon habitat on another. Keywords Mangrove. Seagrass. Tidal marsh. Carbon. Seascape. Sequestration 'When we try to pick out anything by itself, we find it hitched to everything else in the Universe' (John Muir) My first summer in the Sierra,